2004PubMedRequires access

Cardiac amyloidosis presenting as pseudo-hypertrophic cardiomyopathy.

Alexander Papachan, Karen Sliwa, A. Gildenhuys, Rafique Essop

Open publisher page 3 citations

Abstract

Both cardiac amyloidosis and hypertrophic cardiomyopathy may result in excessive hypertrophy of the myocardium, which can be seen on echocardiography. While in most patients the two conditions are easily differentiated, we present in this report a case of amyloidosis that mimicked hypertrophic cardiomyopathy so closely that it required endomyocardial biopsy to establish the diagnosis.

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What this paper is about

Both cardiac amyloidosis and hypertrophic cardiomyopathy may result in excessive hypertrophy of the myocardium, which can be seen on echocardiography. While in most patients the two conditions are easily differentiated, we present in this report a case of amyloidosis that mimicked hypertrophic cardiomyopathy so closely that it required endomyocardial biopsy to establish the diagnosis.

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OpenAlex reports 3 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

Both cardiac amyloidosis and hypertrophic cardiomyopathy may result in excessive hypertrophy of the myocardium, which can be seen on echocardiography. While in most patients the two conditions are easily differentiated, we present in this report a case of amyloidosis that mimicked hypertrophic cardiomyopathy so closely that it required endomyocardial biopsy to establish the diagnosis.

Key concepts: Hypertrophic cardiomyopathy, Endomyocardial biopsy, Cardiac amyloidosis, Medicine, Amyloidosis, Restrictive cardiomyopathy, Cardiology, Cardiomyopathy

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